Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587778720
rs587778720
25 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs587782664
rs587782664
14 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs730882005
rs730882005
20 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs730882008
rs730882008
22 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs786201059
rs786201059
19 0.701 0.360 17 7673764 stop gained C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs863224451
rs863224451
19 0.701 0.440 17 7673796 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs985033810
rs985033810
16 0.724 0.280 17 7674232 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs193920774
rs193920774
21 0.695 0.440 17 7673823 missense variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs587781288
rs587781288
15 0.732 0.440 17 7675190 missense variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs587781991
rs587781991
14 0.724 0.240 17 7675208 missense variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs786202962
rs786202962
17 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
18 0.701 0.360 17 7675095 missense variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs587780071
rs587780071
11 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs121912651
rs121912651
37 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs138729528
rs138729528
25 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 0.700 1.000 1 2016 2016
dbSNP: rs28934574
rs28934574
27 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs397516436
rs397516436
26 0.641 0.440 17 7674894 stop gained G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs121913343
rs121913343
29 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 0.710 1.000 1 2016 2016
dbSNP: rs17849781
rs17849781
14 0.701 0.480 17 7673788 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs28934573
rs28934573
24 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs28934874
rs28934874
21 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs587780070
rs587780070
23 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs786201057
rs786201057
24 0.677 0.400 17 7675995 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs876658468
rs876658468
22 0.689 0.440 17 7674954 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs876659802
rs876659802
15 0.732 0.440 17 7673787 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016